Genome-wide Light-inducible Tuning of Transcriptional Network Dynamic

转录网络动态的全基因组光诱导调节

• 批准号: 8268463
• 负责人: Paola Arlotta
• 金额: $ 65.8万
• 依托单位: HARVARD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-09-27 至 2015-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8268463
• 关键词: Adult; Amyotrophic Lateral Sclerosis; Binding; Biological Sciences; Biology; Brain; Cells; Collection; Color; Communities; Complex; Cues; DNA Binding Domain; DNA Sequence; DNA-Binding Proteins; Development; Disease; Engineering; Etiology; Feedback; Gene Expression; Gene Expression Profile; Gene Expression Regulation; Generations; Genes; Genetic; Genome; Genomics; Goals; Heterogeneity; Histocompatibility Testing; Hour; In Vitro; Individual; Investigation; Light; Link; Mammalian Cell; Maps; Mediating; Medicine; Mental disorders; Methods; Modification; Motor Neurons; Natural regeneration; Nerve Degeneration; Nervous system structure; Neuraxis; Neurodegenerative Disorders; Neurons; Optics; Organism; Physiology; Plants; Play; Population; Protein Engineering; Regenerative Medicine; Regulation; Regulator Genes; Role; Series; Spinal cord injury; Staging; Structure; Techniques; Technology; Testing; Time; Tissues; Work; Zinc Fingers; assay development; biological research; cell type; cellular development; clinically relevant; developmental neurobiology; gene interaction; genome-wide; high throughput screening; improved; in vivo; infancy; injured; interest; microbial; neural circuit; neuron development; new technology; novel; repaired; research study; synthetic biology; technology development

DESCRIPTION (provided by applicant): We propose to develop and apply a paradigm-shifting technological platform that uses a series of Light- Inducible Transcriptional Effectors (LITEs) to orchestrate the temporal regulation of multiple genes in both individual cells in vitro and in the intact organism. The technology we propose to develop will be very broadly applicable and has the potential to radically transform the scale and rate of discovery across different biomedical fields. Application of this novel technology will enable high throughput discovery of the upstream transcriptional regulatory elements of any endogenous gene, as well as temporally precise modulation of gene expression in the native genome. Precise temporal and spatial patterns of gene expression are observed in different tissue and cell types, and are orchestrated and maintained by complex transcriptionally regulated circuits involving multiple genes. Due to the lack of integrated control and readout technologies that enable simultaneous perturbation and "fast" tuning of multiple genes, our ability to causally link transcriptional network dynamics with physiology and development remains at the infancy stage. The LITEs platform will enable modification and regulation of gene expression on the time-scale of hours using a non-invasive, light-mediated inductive strategy, thereby enabling a new generation of interactive genetic studies currently inaccessible with conventional techniques. Our proposal consists of two main components: 1) Novel technology development of light sensitive designer zinc finger (ZF) transcriptional modulators (LITEs-ZF). Genomic, synthetic biology, and protein engineering approaches will be used to develop a suite of novel light-inducible transcriptional regulators targeted at specific genes in the native genome of mammalian cells. Since ZF DNA binding domains can be engineered to target any DNA sequence, ZF-LITEs are applicable to a broad range of biological research studies in a variety of different organisms and cells types. 2) Application of the technology toward high-throughput in vitro and in vivo interrogation of transcriptional network dynamics in the central nervous system. In vitro application will be aimed at identification of upstream effectors of gene expression critical to the differentiation of corticospinal motor neurons (CSMN), a clinically relevant neuronal population that degenerates in amyotrophic lateral sclerosis (ALS) and is injured in spinal cord injury. In vivo application will be focused on directing the regeneration of CSMN by mimicking specific temporal sequences of CSMN-specific developmental cues within the adult brain. Given the broad applicability of this technology, the impact of this proposed work will be far reaching and will radically transform existing experimental approaches for studying gene interactions in all fields of life science and medicine.

描述（由申请人提供）：我们建议开发和应用一种范式转换的技术平台，该平台使用一系列光诱导转录效应器（LITE）来协调体外单个细胞和完整生物体中多个基因的时间调节。我们建议开发的技术将具有非常广泛的适用性，并有可能从根本上改变不同生物医学领域的发现规模和速度。这项新技术的应用将使任何内源基因的上游转录调控元件的高通量发现，以及本地基因组中基因表达的时间精确调节成为可能。在不同的组织和细胞类型中观察到基因表达的精确时间和空间模式，并由涉及多个基因的复杂转录调节回路精心策划和维持。由于缺乏能够同时扰动和“快速”调节多个基因的集成控制和读出技术，我们将转录网络动态与生理学和发育因果联系起来的能力仍处于起步阶段。 LITEs 平台将利用非侵入性、光介导的诱导策略，在数小时的时间尺度上修改和调节基因表达，从而实现目前传统技术无法实现的新一代交互式遗传研究。我们的提案包括两个主要部分：1）光敏设计师锌指（ZF）转录调节剂（LITEs-ZF）的新技术开发。基因组、合成生物学和蛋白质工程方法将用于开发一套针对哺乳动物细胞天然基因组中特定基因的新型光诱导转录调节因子。由于 ZF DNA 结合域可以设计为靶向任何 DNA 序列，因此 ZF-LITE 适用于各种不同生物体和细胞类型的广泛生物学研究。 2）应用该技术对中枢神经系统转录网络动态进行高通量体外和体内询问。体外应用的目的是鉴定对皮质脊髓运动神经元（CSMN）分化至关重要的基因表达上游效应子，CSMN是一种临床相关的神经元群体，在肌萎缩侧索硬化症（ALS）中退化并在脊髓损伤中受损。体内应用将侧重于通过模仿成人大脑内 CSMN 特异性发育线索的特定时间序列来指导 CSMN 的再生。鉴于这项技术的广泛适用性，这项拟议工作的影响将是深远的，并将从根本上改变生命科学和医学所有领域研究基因相互作用的现有实验方法。